Inhibition and Destruction of the Microbial Cell 1971
DOI: 10.1016/b978-0-12-361150-5.50021-3
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The Destruction of Bacterial Spores

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Cited by 109 publications
(162 citation statements)
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“…Their viability at 80 o C was 94.6 % after 10 minutes and 85.7 % after one hour, showing that the spores may be desiccated in spray dryers and pelletized (10) without appreciable loss of viability. Russel (15) showed that D values increased 10 fold every 10 o C fall in temperature; therefore, it may be expected that at temperatures at which the probiotic is stored, the loss in viability shall be inexpressive (17), as it was confirmed by our observations after several months of storage (data not shown). Heat activation was detected after heating at 50 o C during 96 hours.…”
supporting
confidence: 77%
“…Their viability at 80 o C was 94.6 % after 10 minutes and 85.7 % after one hour, showing that the spores may be desiccated in spray dryers and pelletized (10) without appreciable loss of viability. Russel (15) showed that D values increased 10 fold every 10 o C fall in temperature; therefore, it may be expected that at temperatures at which the probiotic is stored, the loss in viability shall be inexpressive (17), as it was confirmed by our observations after several months of storage (data not shown). Heat activation was detected after heating at 50 o C during 96 hours.…”
supporting
confidence: 77%
“…However, aspartate-O-methyltransferase appears to be absent from at least B. subtilis (63), and methionine sulfoxide reductase plays no role in spore resistance to wet heat or oxidizing agents (62). Many workers have noted that spore recovery after a killing treatment (usually wet heat) is often much greater on rich media than on poor media, and this difference has been ascribed to the need for some type of protein "repair" in order for spore outgrowth and eventual colony formation on a poor medium (168,169). Indeed, the heat shock proteins, which play a major role in the resistance of growing cells to heat stress (64a), have been suggested to play a role in spore heat resistance (174), but more recent work has indicated that this is not the case (112a; E. Melly and P. Setlow, unpublished).…”
Section: Parameters Contributing To Spore Resistancementioning
confidence: 99%
“…Initially we examined the disruption of the spore's inner-membrane permeability barrier, as this can accompany spore killing by wet heat (Russell, 1982). However, analysis of decoated dormant spores killed by PON indicated that the major small molecule found in the spore core, DPA, was not released by PON treatment (Table 2).…”
Section: (96) 92 93mentioning
confidence: 99%
“…A number of studies have shown that PON can kill and mutagenize growing bacteria (Brunnelli et al, 1995 ;Hurst & Lymar, 1997 ;Kuwahara et al, 2000 ;Routledge, 2000). However, no such studies have been carried out with bacterial endospores, which are generally much more resistant than growing bacteria to toxic chemicals (Russell, 1982(Russell, , 1990Bloomfield & Arthur, 1994 ;McDonnell & Russell, 1999 ;. Another reason for analysis of the effect of PON on spores is recent work showing that a major route for infection with spores of a human pathogen, Bacillus anthracis, is via uptake and subsequent germination of spores of this organism within alveolar macrophages, cells which can generate PON (Guidi-Rontani et al, 1999).…”
Section: Introductionmentioning
confidence: 99%